Clinical Trial Associate

Clinical Careers Page(20 days ago)

Burlington, CanadaOnsiteFull TimeSenior$102,905 - $140,558 (estimated)Clinical Operations

About this role

A Clinical Trial Associate at ICON plays a vital role in overseeing site management activities for clinical trials, ensuring compliance with regulations and timely data collection. The role involves collaborating with site staff and teams to support the smooth operation of clinical studies and ensuring study goals are met.

View Original Listing

Required Skills

Clinical Trials
Site Management
GCP
Regulatory Compliance
Data Collection
Monitoring
Clinical Operations
Problem Solving
Organizational Skills
Communication

About Clinical Careers Page

iconplc.com

ICON plc is a global clinical research organisation (CRO) that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies. It offers end-to-end drug and device development support — including clinical trial management across phases, data management and biostatistics, regulatory and safety/pharmacovigilance, and commercialisation and market-access services. ICON combines scientific and therapeutic expertise with technology and a scalable global operations network to accelerate development and bring therapies to patients. Clients engage ICON for integrated, experienced CRO support across the full product lifecycle.

View more jobs at Clinical Careers Page →